Genes and Development

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


GENES & DEVELOPMENT 18:1606-1617, 2004
©2004 by Cold Spring Harbor Laboratory Press; ISSN 0890-9369/ $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lim, C. Y.
Right arrow Articles by Kadonaga, J. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lim, C. Y.
Right arrow Articles by Kadonaga, J. T.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

RESEARCH PAPER

The MTE, a new core promoter element for transcription by RNA polymerase II

Chin Yan Lim1, Buyung Santoso1, Thomas Boulay1, Emily Dong1, Uwe Ohler2 and James T. Kadonaga1,3

1 Section of Molecular Biology, University of California at San Diego, La Jolla, California 92093, USA; 2 Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA

The core promoter is the ultimate target of the vast network of regulatory factors that contribute to the initiation of transcription by RNA polymerase II. Here we describe the MTE (motif ten element), a new core promoter element that appears to be conserved from Drosophila to humans. The MTE promotes transcription by RNA polymerase II when it is located precisely at positions +18 to +27 relative to A+1 in the initiator (Inr) element. MTE sequences from +18 to +22 relative to A+1 are important for basal transcription, and a region from +18 to +27 is sufficient to confer MTE activity to heterologous core promoters. The MTE requires the Inr, but functions independently of the TATA-box and DPE. Notably, the loss of transcriptional activity upon mutation of a TATA-box or DPE can be compensated by the addition of an MTE. In addition, the MTE exhibits strong synergism with the TATA-box as well as the DPE. These findings indicate that the MTE is a novel downstream core promoter element that is important for transcription by RNA polymerase II.

[Keywords: RNA polymerase II; core promoter; DPE; Inr; TATA-box]

Received February 11, 2004; revised version accepted April 30, 2004.


Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.1193404.

3 Corresponding author. E-MAIL jkadonaga{at}ucsd.edu; FAX (858) 534-0555.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
D. A. Hendrix, J.-W. Hong, J. Zeitlinger, D. S. Rokhsar, and M. S. Levine
Promoter elements associated with RNA Pol II stalling in the Drosophila embryo
PNAS, June 3, 2008; 105(22): 7762 - 7767.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
M. Hackenberg and R. Matthiesen
Annotation-Modules: a tool for finding significant combinations of multisource annotations for gene lists
Bioinformatics, June 1, 2008; 24(11): 1386 - 1393.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
C. Lee, X. Li, A. Hechmer, M. Eisen, M. D. Biggin, B. J. Venters, C. Jiang, J. Li, B. F. Pugh, and D. S. Gilmour
NELF and GAGA Factor Are Linked to Promoter-Proximal Pausing at Many Genes in Drosophila
Mol. Cell. Biol., May 15, 2008; 28(10): 3290 - 3300.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P. Kundu, A. Alioua, E. Stefani, and L. Toro
Regulation of Mouse Slo Gene Expression: MULTIPLE PROMOTERS, TRANSCRIPTION START SITES, AND GENOMIC ACTION OF ESTROGEN
J. Biol. Chem., September 14, 2007; 282(37): 27478 - 27492.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
H. Xi, Y. Yu, Y. Fu, J. Foley, A. Halees, and Z. Weng
Analysis of overrepresented motifs in human core promoters reveals dual regulatory roles of YY1
Genome Res., June 1, 2007; 17(6): 798 - 806.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
S. Vardhanabhuti, J. Wang, and S. Hannenhalli
Position and distance specificity are important determinants of cis-regulatory motifs in addition to evolutionary conservation
Nucleic Acids Res., May 11, 2007; 35(10): 3203 - 3213.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
Y. Tokusumi, Y. Ma, X. Song, R. H. Jacobson, and S. Takada
The New Core Promoter Element XCPE1 (X Core Promoter Element 1) Directs Activator-, Mediator-, and TATA-Binding Protein-Dependent but TFIID-Independent RNA Polymerase II Transcription from TATA-Less Promoters
Mol. Cell. Biol., March 1, 2007; 27(5): 1844 - 1858.
[Abstract] [Full Text] [PDF]


Home page
Eukaryot CellHome page
I. Skovorodkin, A. Pimenov, I. Raykhel, B. Schimanski, D. Ammermann, and A. Gunzl
{alpha}-Tubulin Minichromosome Promoters in the Stichotrichous Ciliate Stylonychia lemnae
Eukaryot. Cell, January 1, 2007; 6(1): 28 - 36.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
U. Ohler
Identification of core promoter modules in Drosophila and their application in accurate transcription start site prediction
Nucleic Acids Res., November 6, 2006; 34(20): 5943 - 5950.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
D.-H. Lee, N. Gershenzon, M. Gupta, I. P. Ioshikhes, D. Reinberg, and B. A. Lewis
Functional Characterization of Core Promoter Elements: the Downstream Core Element Is Recognized by TAF1
Mol. Cell. Biol., November 1, 2005; 25(21): 9674 - 9686.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
W. Deng and S. G.E. Roberts
A core promoter element downstream of the TATA box that is recognized by TFIIB
Genes & Dev., October 15, 2005; 19(20): 2418 - 2423.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
P. G. Gallagher, D. G. Nilson, C. Wong, J. L. Weisbein, L. J. Garrett-Beal, S. W. Eber, and D. M. Bodine
A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosis
Hum. Mol. Genet., September 1, 2005; 14(17): 2501 - 2509.
[Abstract] [Full Text] [PDF]


Home page
J BiochemHome page
T. T. T. Le, S. Zhang, N. Hayashi, M. Yasukawa, L. Delgermaa, and S. Murakami
Mutational Analysis of Human RNA Polymerase II Subunit 5 (RPB5): The Residues Critical for Interactions with TFIIF Subunit RAP30 and Hepatitis B Virus X Protein
J. Biochem., September 1, 2005; 138(3): 215 - 224.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
J. Wang, J. Zhang, H. Jiang, C. Liu, F. Yi, and Y. Hu
Nucleotide sequence and genomic organization of a newly isolated densovirus infecting Dendrolimus punctatus
J. Gen. Virol., August 1, 2005; 86(8): 2169 - 2173.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Genome Res. Learn. Mem.
Protein Science RNA Genes Dev.
Copyright © 2004 by Cold Spring Harbor Laboratory Press.